Other mutations in this stock |
Total: 75 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abhd12b |
T |
A |
12: 70,206,221 (GRCm39) |
N67K |
probably benign |
Het |
Amotl1 |
C |
A |
9: 14,556,216 (GRCm39) |
E37* |
probably null |
Het |
Ap4b1 |
C |
A |
3: 103,720,601 (GRCm39) |
Y90* |
probably null |
Het |
Atl1 |
T |
A |
12: 69,972,813 (GRCm39) |
H44Q |
probably damaging |
Het |
Atp6v0b |
G |
A |
4: 117,742,864 (GRCm39) |
T74M |
probably benign |
Het |
Auts2 |
T |
C |
5: 131,469,437 (GRCm39) |
T627A |
probably benign |
Het |
B4galnt4 |
T |
A |
7: 140,647,449 (GRCm39) |
I372N |
possibly damaging |
Het |
B4galt2 |
A |
G |
4: 117,731,148 (GRCm39) |
S338P |
probably damaging |
Het |
Cfap43 |
A |
C |
19: 47,773,717 (GRCm39) |
|
probably null |
Het |
Col4a1 |
T |
C |
8: 11,362,538 (GRCm39) |
|
probably benign |
Het |
Col7a1 |
A |
C |
9: 108,798,494 (GRCm39) |
I1741L |
possibly damaging |
Het |
Coprs |
A |
T |
8: 13,935,750 (GRCm39) |
S90T |
probably benign |
Het |
Csrnp3 |
T |
C |
2: 65,779,408 (GRCm39) |
V40A |
possibly damaging |
Het |
Ephx1 |
C |
A |
1: 180,827,287 (GRCm39) |
|
probably null |
Het |
Erich6 |
C |
A |
3: 58,526,220 (GRCm39) |
R594L |
probably benign |
Het |
F2rl2 |
A |
T |
13: 95,837,038 (GRCm39) |
N28Y |
probably damaging |
Het |
Fbxo38 |
A |
T |
18: 62,639,740 (GRCm39) |
N1041K |
possibly damaging |
Het |
Fcgr2b |
C |
T |
1: 170,790,977 (GRCm39) |
|
probably null |
Het |
Fsip2 |
T |
A |
2: 82,809,061 (GRCm39) |
N1793K |
probably damaging |
Het |
Gatad1 |
T |
C |
5: 3,693,540 (GRCm39) |
R210G |
probably benign |
Het |
Gcnt3 |
A |
G |
9: 69,942,169 (GRCm39) |
I133T |
probably damaging |
Het |
Gm57859 |
A |
G |
11: 113,578,818 (GRCm39) |
D71G |
probably benign |
Het |
Hoxa1 |
T |
A |
6: 52,135,021 (GRCm39) |
I61F |
probably damaging |
Het |
Impact |
C |
T |
18: 13,115,169 (GRCm39) |
L102F |
probably damaging |
Het |
Ist1 |
A |
T |
8: 110,404,284 (GRCm39) |
I196N |
probably damaging |
Het |
Kcnv2 |
T |
A |
19: 27,311,282 (GRCm39) |
S550T |
probably benign |
Het |
Krt1c |
A |
T |
15: 101,726,314 (GRCm39) |
S75T |
unknown |
Het |
Krtap21-1 |
A |
G |
16: 89,200,466 (GRCm39) |
S59P |
unknown |
Het |
Lef1 |
A |
T |
3: 130,905,223 (GRCm39) |
I35F |
probably damaging |
Het |
Lpcat2 |
A |
C |
8: 93,599,707 (GRCm39) |
N225T |
probably damaging |
Het |
Lztfl1 |
A |
T |
9: 123,538,649 (GRCm39) |
N142K |
probably benign |
Het |
Mdh1b |
G |
A |
1: 63,760,975 (GRCm39) |
H88Y |
probably benign |
Het |
Mettl26 |
A |
G |
17: 26,095,658 (GRCm39) |
D171G |
probably damaging |
Het |
Mrps24 |
A |
T |
11: 5,654,663 (GRCm39) |
M97K |
probably benign |
Het |
Ms4a14 |
A |
T |
19: 11,279,499 (GRCm39) |
C1020S |
probably benign |
Het |
Mterf1a |
A |
T |
5: 3,940,854 (GRCm39) |
I338K |
probably benign |
Het |
Odad2 |
A |
T |
18: 7,294,479 (GRCm39) |
Y45N |
probably benign |
Het |
Or1e22 |
A |
G |
11: 73,377,299 (GRCm39) |
I117T |
probably benign |
Het |
Or4p20 |
T |
C |
2: 88,254,156 (GRCm39) |
Y71C |
possibly damaging |
Het |
Or52s1b |
T |
A |
7: 102,822,442 (GRCm39) |
H134L |
probably damaging |
Het |
Or7g12 |
T |
A |
9: 18,899,689 (GRCm39) |
I135N |
probably damaging |
Het |
Paqr3 |
T |
A |
5: 97,256,146 (GRCm39) |
H76L |
probably damaging |
Het |
Parp1 |
T |
A |
1: 180,417,071 (GRCm39) |
Y618* |
probably null |
Het |
Pilrb2 |
C |
T |
5: 137,870,049 (GRCm39) |
|
probably benign |
Het |
Pkm |
A |
G |
9: 59,575,853 (GRCm39) |
N90D |
probably damaging |
Het |
Pla2g4c |
T |
G |
7: 13,078,459 (GRCm39) |
|
probably null |
Het |
Plppr4 |
C |
T |
3: 117,116,667 (GRCm39) |
V339I |
probably damaging |
Het |
Pnkp |
T |
A |
7: 44,510,462 (GRCm39) |
D304E |
probably damaging |
Het |
Pnlip |
T |
C |
19: 58,668,067 (GRCm39) |
|
probably null |
Het |
Polr2a |
A |
G |
11: 69,638,026 (GRCm39) |
C148R |
probably damaging |
Het |
Ppp1r10 |
G |
A |
17: 36,240,443 (GRCm39) |
G578S |
probably benign |
Het |
Ptges2 |
C |
T |
2: 32,287,683 (GRCm39) |
T137I |
possibly damaging |
Het |
Ptpre |
T |
C |
7: 135,270,877 (GRCm39) |
V344A |
possibly damaging |
Het |
Rag1 |
A |
G |
2: 101,472,137 (GRCm39) |
F1002L |
probably damaging |
Het |
Rcn2 |
T |
A |
9: 55,960,298 (GRCm39) |
Y188* |
probably null |
Het |
Rest |
A |
G |
5: 77,416,046 (GRCm39) |
S87G |
probably damaging |
Het |
Rgsl1 |
C |
T |
1: 153,675,568 (GRCm39) |
D913N |
probably damaging |
Het |
Scp2 |
A |
G |
4: 107,928,475 (GRCm39) |
M1T |
probably null |
Het |
Slamf8 |
T |
A |
1: 172,415,590 (GRCm39) |
N83Y |
probably damaging |
Het |
Slc26a11 |
T |
A |
11: 119,248,844 (GRCm39) |
F75Y |
possibly damaging |
Het |
Slc26a5 |
A |
G |
5: 22,045,570 (GRCm39) |
S133P |
probably damaging |
Het |
Sncb |
A |
T |
13: 54,910,487 (GRCm39) |
V83E |
probably damaging |
Het |
Tmem243 |
A |
G |
5: 9,151,348 (GRCm39) |
T11A |
probably damaging |
Het |
Trim38 |
A |
G |
13: 23,973,502 (GRCm39) |
N277D |
probably benign |
Het |
Vmn1r189 |
C |
T |
13: 22,286,628 (GRCm39) |
G70S |
probably damaging |
Het |
Vmn2r-ps117 |
A |
G |
17: 19,058,495 (GRCm39) |
R684G |
probably benign |
Het |
Wdr59 |
T |
C |
8: 112,187,420 (GRCm39) |
N792D |
possibly damaging |
Het |
Wnt5a |
A |
G |
14: 28,244,527 (GRCm39) |
D238G |
possibly damaging |
Het |
Zbtb42 |
C |
A |
12: 112,646,824 (GRCm39) |
T333K |
probably damaging |
Het |
Zfp119b |
A |
G |
17: 56,245,564 (GRCm39) |
S509P |
probably benign |
Het |
Zfp365 |
T |
A |
10: 67,745,594 (GRCm39) |
K61N |
probably damaging |
Het |
Zfp553 |
T |
C |
7: 126,835,825 (GRCm39) |
F460S |
probably damaging |
Het |
Zfp788 |
C |
T |
7: 41,299,301 (GRCm39) |
Q594* |
probably null |
Het |
Zfp984 |
T |
A |
4: 147,845,707 (GRCm39) |
M1L |
possibly damaging |
Het |
Zmiz2 |
T |
A |
11: 6,347,566 (GRCm39) |
Y291* |
probably null |
Het |
|
Other mutations in Apc |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00507:Apc
|
APN |
18 |
34,449,979 (GRCm39) |
missense |
probably benign |
0.01 |
IGL00898:Apc
|
APN |
18 |
34,450,147 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01111:Apc
|
APN |
18 |
34,448,189 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL01347:Apc
|
APN |
18 |
34,450,723 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01375:Apc
|
APN |
18 |
34,446,707 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01805:Apc
|
APN |
18 |
34,451,271 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01997:Apc
|
APN |
18 |
34,448,476 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02033:Apc
|
APN |
18 |
34,443,772 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02323:Apc
|
APN |
18 |
34,448,863 (GRCm39) |
nonsense |
probably null |
|
IGL02373:Apc
|
APN |
18 |
34,449,212 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02379:Apc
|
APN |
18 |
34,431,798 (GRCm39) |
missense |
probably benign |
0.45 |
IGL02456:Apc
|
APN |
18 |
34,446,935 (GRCm39) |
nonsense |
probably null |
|
IGL02552:Apc
|
APN |
18 |
34,446,035 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL02676:Apc
|
APN |
18 |
34,448,687 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02756:Apc
|
APN |
18 |
34,447,588 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02938:Apc
|
APN |
18 |
34,448,281 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02974:Apc
|
APN |
18 |
34,401,436 (GRCm39) |
splice site |
probably benign |
|
IGL03124:Apc
|
APN |
18 |
34,433,038 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03201:Apc
|
APN |
18 |
34,445,429 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03339:Apc
|
APN |
18 |
34,431,527 (GRCm39) |
missense |
probably damaging |
1.00 |
FR4304:Apc
|
UTSW |
18 |
34,415,050 (GRCm39) |
intron |
probably benign |
|
FR4342:Apc
|
UTSW |
18 |
34,415,052 (GRCm39) |
intron |
probably benign |
|
FR4449:Apc
|
UTSW |
18 |
34,415,058 (GRCm39) |
intron |
probably benign |
|
FR4449:Apc
|
UTSW |
18 |
34,415,053 (GRCm39) |
intron |
probably benign |
|
FR4548:Apc
|
UTSW |
18 |
34,415,051 (GRCm39) |
intron |
probably benign |
|
FR4737:Apc
|
UTSW |
18 |
34,415,052 (GRCm39) |
intron |
probably benign |
|
FR4976:Apc
|
UTSW |
18 |
34,415,057 (GRCm39) |
nonsense |
probably null |
|
FR4976:Apc
|
UTSW |
18 |
34,415,053 (GRCm39) |
intron |
probably benign |
|
FR4976:Apc
|
UTSW |
18 |
34,415,051 (GRCm39) |
intron |
probably benign |
|
R0385:Apc
|
UTSW |
18 |
34,448,997 (GRCm39) |
missense |
probably damaging |
1.00 |
R0535:Apc
|
UTSW |
18 |
34,394,125 (GRCm39) |
missense |
probably damaging |
1.00 |
R0561:Apc
|
UTSW |
18 |
34,446,356 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0590:Apc
|
UTSW |
18 |
34,449,283 (GRCm39) |
nonsense |
probably null |
|
R0626:Apc
|
UTSW |
18 |
34,451,507 (GRCm39) |
missense |
probably damaging |
1.00 |
R0991:Apc
|
UTSW |
18 |
34,449,160 (GRCm39) |
missense |
probably damaging |
1.00 |
R1564:Apc
|
UTSW |
18 |
34,448,202 (GRCm39) |
missense |
probably benign |
0.00 |
R1663:Apc
|
UTSW |
18 |
34,401,378 (GRCm39) |
missense |
probably damaging |
0.98 |
R1737:Apc
|
UTSW |
18 |
34,450,075 (GRCm39) |
missense |
probably damaging |
1.00 |
R1739:Apc
|
UTSW |
18 |
34,445,371 (GRCm39) |
missense |
probably damaging |
1.00 |
R1835:Apc
|
UTSW |
18 |
34,450,130 (GRCm39) |
missense |
probably damaging |
1.00 |
R1887:Apc
|
UTSW |
18 |
34,405,521 (GRCm39) |
missense |
probably damaging |
1.00 |
R1957:Apc
|
UTSW |
18 |
34,450,388 (GRCm39) |
missense |
probably damaging |
1.00 |
R1974:Apc
|
UTSW |
18 |
34,433,057 (GRCm39) |
missense |
possibly damaging |
0.62 |
R2005:Apc
|
UTSW |
18 |
34,443,962 (GRCm39) |
critical splice donor site |
probably null |
|
R2013:Apc
|
UTSW |
18 |
34,448,644 (GRCm39) |
missense |
probably damaging |
0.98 |
R2014:Apc
|
UTSW |
18 |
34,448,644 (GRCm39) |
missense |
probably damaging |
0.98 |
R2015:Apc
|
UTSW |
18 |
34,448,644 (GRCm39) |
missense |
probably damaging |
0.98 |
R2017:Apc
|
UTSW |
18 |
34,446,655 (GRCm39) |
missense |
probably benign |
0.00 |
R2056:Apc
|
UTSW |
18 |
34,449,481 (GRCm39) |
missense |
probably damaging |
1.00 |
R2108:Apc
|
UTSW |
18 |
34,402,282 (GRCm39) |
missense |
probably damaging |
1.00 |
R2120:Apc
|
UTSW |
18 |
34,409,654 (GRCm39) |
missense |
probably damaging |
1.00 |
R2131:Apc
|
UTSW |
18 |
34,445,098 (GRCm39) |
missense |
possibly damaging |
0.51 |
R2133:Apc
|
UTSW |
18 |
34,445,098 (GRCm39) |
missense |
possibly damaging |
0.51 |
R2291:Apc
|
UTSW |
18 |
34,445,544 (GRCm39) |
missense |
probably benign |
0.45 |
R2332:Apc
|
UTSW |
18 |
34,450,112 (GRCm39) |
missense |
possibly damaging |
0.50 |
R2360:Apc
|
UTSW |
18 |
34,394,179 (GRCm39) |
missense |
probably damaging |
1.00 |
R2407:Apc
|
UTSW |
18 |
34,447,315 (GRCm39) |
missense |
possibly damaging |
0.77 |
R2507:Apc
|
UTSW |
18 |
34,449,590 (GRCm39) |
missense |
possibly damaging |
0.77 |
R2940:Apc
|
UTSW |
18 |
34,409,723 (GRCm39) |
missense |
probably damaging |
1.00 |
R3404:Apc
|
UTSW |
18 |
34,446,655 (GRCm39) |
missense |
probably benign |
0.00 |
R3411:Apc
|
UTSW |
18 |
34,402,312 (GRCm39) |
splice site |
probably benign |
|
R3778:Apc
|
UTSW |
18 |
34,446,134 (GRCm39) |
missense |
probably damaging |
1.00 |
R3826:Apc
|
UTSW |
18 |
34,412,388 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4599:Apc
|
UTSW |
18 |
34,451,040 (GRCm39) |
nonsense |
probably null |
|
R4611:Apc
|
UTSW |
18 |
34,451,618 (GRCm39) |
missense |
probably damaging |
1.00 |
R4664:Apc
|
UTSW |
18 |
34,431,647 (GRCm39) |
missense |
probably damaging |
0.98 |
R4969:Apc
|
UTSW |
18 |
34,445,971 (GRCm39) |
nonsense |
probably null |
|
R5007:Apc
|
UTSW |
18 |
34,446,016 (GRCm39) |
missense |
probably damaging |
1.00 |
R5066:Apc
|
UTSW |
18 |
34,449,158 (GRCm39) |
missense |
probably damaging |
1.00 |
R5112:Apc
|
UTSW |
18 |
34,449,162 (GRCm39) |
nonsense |
probably null |
|
R5259:Apc
|
UTSW |
18 |
34,447,343 (GRCm39) |
missense |
probably benign |
0.29 |
R5440:Apc
|
UTSW |
18 |
34,354,213 (GRCm39) |
unclassified |
probably benign |
|
R5508:Apc
|
UTSW |
18 |
34,431,633 (GRCm39) |
missense |
probably damaging |
0.97 |
R5512:Apc
|
UTSW |
18 |
34,443,962 (GRCm39) |
critical splice donor site |
probably benign |
|
R5850:Apc
|
UTSW |
18 |
34,451,116 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5951:Apc
|
UTSW |
18 |
34,450,199 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5966:Apc
|
UTSW |
18 |
34,354,140 (GRCm39) |
utr 5 prime |
probably benign |
|
R6081:Apc
|
UTSW |
18 |
34,423,164 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6116:Apc
|
UTSW |
18 |
34,449,508 (GRCm39) |
missense |
probably damaging |
1.00 |
R6351:Apc
|
UTSW |
18 |
34,445,265 (GRCm39) |
missense |
probably damaging |
1.00 |
R6354:Apc
|
UTSW |
18 |
34,445,581 (GRCm39) |
missense |
probably benign |
0.02 |
R6467:Apc
|
UTSW |
18 |
34,402,252 (GRCm39) |
missense |
probably benign |
0.22 |
R7027:Apc
|
UTSW |
18 |
34,445,129 (GRCm39) |
missense |
probably damaging |
1.00 |
R7096:Apc
|
UTSW |
18 |
34,449,010 (GRCm39) |
missense |
probably damaging |
1.00 |
R7289:Apc
|
UTSW |
18 |
34,448,324 (GRCm39) |
missense |
probably damaging |
1.00 |
R7439:Apc
|
UTSW |
18 |
34,445,126 (GRCm39) |
missense |
probably damaging |
1.00 |
R7441:Apc
|
UTSW |
18 |
34,445,126 (GRCm39) |
missense |
probably damaging |
1.00 |
R7534:Apc
|
UTSW |
18 |
34,450,015 (GRCm39) |
missense |
probably damaging |
1.00 |
R7685:Apc
|
UTSW |
18 |
34,447,261 (GRCm39) |
missense |
probably damaging |
1.00 |
R7814:Apc
|
UTSW |
18 |
34,405,592 (GRCm39) |
missense |
probably damaging |
0.98 |
R7954:Apc
|
UTSW |
18 |
34,447,321 (GRCm39) |
missense |
probably damaging |
0.99 |
R8352:Apc
|
UTSW |
18 |
34,445,804 (GRCm39) |
missense |
possibly damaging |
0.54 |
R8452:Apc
|
UTSW |
18 |
34,445,804 (GRCm39) |
missense |
possibly damaging |
0.54 |
R8497:Apc
|
UTSW |
18 |
34,446,083 (GRCm39) |
missense |
possibly damaging |
0.81 |
R8545:Apc
|
UTSW |
18 |
34,450,084 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8554:Apc
|
UTSW |
18 |
34,445,999 (GRCm39) |
missense |
probably damaging |
1.00 |
R8955:Apc
|
UTSW |
18 |
34,401,370 (GRCm39) |
missense |
probably damaging |
1.00 |
R9014:Apc
|
UTSW |
18 |
34,354,074 (GRCm39) |
start gained |
probably benign |
|
R9061:Apc
|
UTSW |
18 |
34,446,251 (GRCm39) |
missense |
probably damaging |
1.00 |
R9147:Apc
|
UTSW |
18 |
34,450,710 (GRCm39) |
missense |
probably damaging |
1.00 |
R9318:Apc
|
UTSW |
18 |
34,447,040 (GRCm39) |
missense |
possibly damaging |
0.69 |
R9521:Apc
|
UTSW |
18 |
34,445,738 (GRCm39) |
missense |
probably benign |
0.24 |
R9546:Apc
|
UTSW |
18 |
34,445,311 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9547:Apc
|
UTSW |
18 |
34,445,311 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9557:Apc
|
UTSW |
18 |
34,451,412 (GRCm39) |
missense |
probably damaging |
1.00 |
R9592:Apc
|
UTSW |
18 |
34,443,823 (GRCm39) |
nonsense |
probably null |
|
R9675:Apc
|
UTSW |
18 |
34,449,247 (GRCm39) |
missense |
probably damaging |
1.00 |
R9736:Apc
|
UTSW |
18 |
34,450,823 (GRCm39) |
missense |
probably damaging |
1.00 |
R9792:Apc
|
UTSW |
18 |
34,447,628 (GRCm39) |
missense |
probably damaging |
1.00 |
R9793:Apc
|
UTSW |
18 |
34,447,628 (GRCm39) |
missense |
probably damaging |
1.00 |
R9795:Apc
|
UTSW |
18 |
34,447,628 (GRCm39) |
missense |
probably damaging |
1.00 |
RF046:Apc
|
UTSW |
18 |
34,415,062 (GRCm39) |
critical splice donor site |
probably benign |
|
RF063:Apc
|
UTSW |
18 |
34,415,062 (GRCm39) |
critical splice donor site |
probably benign |
|
X0021:Apc
|
UTSW |
18 |
34,445,161 (GRCm39) |
missense |
probably damaging |
1.00 |
X0025:Apc
|
UTSW |
18 |
34,445,429 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Apc
|
UTSW |
18 |
34,446,220 (GRCm39) |
nonsense |
probably null |
|
Z1177:Apc
|
UTSW |
18 |
34,447,516 (GRCm39) |
missense |
probably benign |
0.06 |
|